Hypothesis: We hypothesize that perfused and total micro vessel density in living kidney donors will be decreased after kidney donation.
ID
Bron
Verkorte titel
Aandoening
Not applicable
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Primary outcome: Mean perfused vessel density difference between different time points will analysed by using paired T-tests.
Achtergrond van het onderzoek
Rationale:
Recent studies comparing equally healthy controls with donors suggest that living kidney donation is associated with increased risk of developing cardiovascular disease. However, mechanisms underlying this possible association remain unknown. In this study, we aim to investigate whether microcirculatory perfusion becomes compromised after unilateral nephrectomy in living donors in order to get more insight in the possible mechanism behind the development of CVD after kidney donation.
Objective:
To study microcirculatory perfusion in living kidney donors before and after donation.
Study design:
Single center, prospective observational study
Study population:
Living kidney donors > 18 years of age.
Intervention (if applicable):
Not applicable
Main study parameters/endpoints:
The primary outcome is to study the difference in perfused and total vessel density before and after unilateral nephrectomy in living kidney donors.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
There will be no benefit for patients participating in this study. The use of the USB3 MicroScan imaging camera is a non-invasive sublingually measurement technique which exposes patients to minimal risk and burden.
Doel van het onderzoek
Hypothesis: We hypothesize that perfused and total micro vessel density in living kidney donors will be decreased after kidney donation.
Onderzoeksopzet
Time points: 1 day before donation and 3 weeks after donation.
Onderzoeksproduct en/of interventie
Not applicable
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Age > 18
- Living kidney donors
- Provision of written informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Exclusion criteria:
- If candidate cannot understand Dutch or English.
Opzet
Deelname
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Toelichting
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In overige registers
Register | ID |
---|---|
NTR-new | NL7566 |
CCMO | NL65200.029.18 |
OMON | NL-OMON46695 |